Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

A/C | Ancestral: A | Ambiguity code: M

Chromosome 15:64162961 (forward strand) | View in location tab

Most severe consequence
Missense variant
Evidence status

Clinical significance


This variant has 2 synonyms - Show

HGVS names

This variant has 8 HGVS names - Show

About this variant

This variant overlaps 6 transcripts, 1 regulatory feature and is associated with 3 phenotypes.

Variant displays